General Chemistry: Atoms First
2nd Edition
ISBN: 9780321809261
Author: John E. McMurry, Robert C. Fay
Publisher: Prentice Hall
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Textbook Question
Chapter 4, Problem 4.30CP
Sinapaldehyde, a compound present in the toasted wood used for aging wine, has the following connections among atoms. Complete the following electron-dot structure for sinapaldehyde, and identify any multiple bonds in the molecule:
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Chapter 4 Solutions
General Chemistry: Atoms First
Ch. 4.2 - Prob. 4.1PCh. 4.2 - Prob. 4.2PCh. 4.2 - Prob. 4.3CPCh. 4.4 - Use the electronegativity values in Figure 4.4 to...Ch. 4.4 - Order the following compounds according to the...Ch. 4.4 - An electrostatic potential map of water is shown...Ch. 4.5 - Prob. 4.7PCh. 4.5 - Write formulas for compounds with the following...Ch. 4.5 - Prob. 4.9CPCh. 4.6 - Draw electron-dot structures for the following...
Ch. 4.6 - Draw an electron-dot structure for the hydronium...Ch. 4.7 - Draw electron-dot structures for the following...Ch. 4.7 - There are two molecules with the formula C2H6O....Ch. 4.7 - The following structure is a representation of...Ch. 4.8 - Carbon monoxide, CO, is a deadly gas produced by...Ch. 4.8 - Draw an electron-dot structure for each of the...Ch. 4.8 - Prob. 4.17PCh. 4.9 - Prob. 4.18PCh. 4.9 - Draw as many resonance structures as possible for...Ch. 4.9 - The following structure shows the connections...Ch. 4.10 - Calculate the formal charge on each atom in the...Ch. 4.10 - Calculate the formal charge on each atom in the...Ch. 4.10 - What is a radical, and why are they so reactive?Ch. 4.10 - Prob. 4.24PCh. 4.10 - Draw an electron-dot structure for the ethyl...Ch. 4 - Two electrostatic potential maps are shown, one of...Ch. 4 - Prob. 4.27CPCh. 4 - Prob. 4.28CPCh. 4 - Prob. 4.29CPCh. 4 - Sinapaldehyde, a compound present in the toasted...Ch. 4 - Vitamin C (ascorbic acid) has the following...Ch. 4 - What general trends in electronegativity occur in...Ch. 4 - Prob. 4.33SPCh. 4 - Prob. 4.34SPCh. 4 - Prob. 4.35SPCh. 4 - Prob. 4.36SPCh. 4 - Prob. 4.37SPCh. 4 - Prob. 4.38SPCh. 4 - Show the direction of polarity for each of the...Ch. 4 - Prob. 4.40SPCh. 4 - Prob. 4.41SPCh. 4 - Prob. 4.42SPCh. 4 - Prob. 4.43SPCh. 4 - Prob. 4.44SPCh. 4 - Prob. 4.45SPCh. 4 - Prob. 4.46SPCh. 4 - Prob. 4.47SPCh. 4 - Prob. 4.48SPCh. 4 - Prob. 4.49SPCh. 4 - Prob. 4.50SPCh. 4 - Which of the following substances contains an atom...Ch. 4 - Draw electron-dot structures for the following...Ch. 4 - Prob. 4.53SPCh. 4 - Oxalic acid, H2C2O4, is a mildly poisonous...Ch. 4 - Draw an electron-dot structure for carbon...Ch. 4 - Prob. 4.56SPCh. 4 - Prob. 4.57SPCh. 4 - Prob. 4.58SPCh. 4 - Prob. 4.59SPCh. 4 - Methylphenidate (C14H19NO2), marketed as Ritalin,...Ch. 4 - Pregabalin (C8H17NO2), marketed as Lyrica, is an...Ch. 4 - Draw as many resonance structures as you can that...Ch. 4 - Prob. 4.63SPCh. 4 - Which of the following pairs of structures...Ch. 4 - Which of the following pairs of structures...Ch. 4 - Draw an electron-dot structure for carbon...Ch. 4 - Prob. 4.67SPCh. 4 - Prob. 4.68SPCh. 4 - Prob. 4.69SPCh. 4 - Prob. 4.70SPCh. 4 - Prob. 4.71SPCh. 4 - Prob. 4.72SPCh. 4 - Prob. 4.73SPCh. 4 - Prob. 4.74CHPCh. 4 - Thiofulminic acid, , is a highly reactive...Ch. 4 - Draw two resonance structures for methyl...Ch. 4 - Prob. 4.78CHPCh. 4 - Prob. 4.79CHPCh. 4 - Prob. 4.80CHPCh. 4 - Prob. 4.81CHPCh. 4 - Prob. 4.82CHPCh. 4 - Prob. 4.83CHPCh. 4 - Prob. 4.84CHPCh. 4 - Prob. 4.85CHPCh. 4 - Sulfur reacts with chlorine to give a product that...Ch. 4 - Sulfur reacts with ammonia to give a product A...Ch. 4 - Prob. 4.88MPCh. 4 - Prob. 4.89MP
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- What aspect of the following Lewis structure indicates that the concept of coordinate covalency is needed to explain the bonding in the molecule?arrow_forward7.18 In terms of the strengths of the covalent bonds involved, why do combustion reactions release energy?arrow_forwardSketch a graph of the potential energy of two atoms as a function of the distance between them. On your graph, indicate how bond energy and bond distance are defined.arrow_forward
- Two Lewis structures can be written for nitrosyl fluoride, which contains one nitrogen, one oxygen, and one fluorine atom per molecule. Write the two Lewis structures land assign a formal charge to each atom.arrow_forwardGiven the bonds C N, C H, C Br, and S O, (a) which atom in each is the more electronegative? (b) which of these bonds is the most polar?arrow_forward7.30 The bond in HF is said to be polar, with the hydrogen carrying a partial positive charge. For this to be true, the hydrogen atom must have less than one electron around it. Yet the Lewis dot structure of HF attributes two electrons to hydrogen. Draw a picture of the electron density distribution for HF and use it to describe how the hydrogen atom can carry a partial positive charge. How can these two models of the HF bond (the electron density and the Lewis structure) seem so different and yet describe the same thing?arrow_forward
- What information can you use to predict whether a bond between two atoms is covalent or ionic?arrow_forwardIn nitryl chloride (NO2Cl), the chlorine atom and the twooxygen atoms are bonded to a central nitrogen atom, andall the atoms lie in a plane. Draw the two electron dot resonance forms that satisfy the octet rule and that together areconsistent with the fact that the two nitrogen–oxygenbonds are equivalent.arrow_forwardEach Lewis structure of benzene has three C“C double bonds. Anotherhydrocarbon containing three C“C double bonds is hexatriene, C6H8. A Lewisstructure of hexatriene is Experiments show that three of the C¬C bonds in hexatriene are shorter than theother two. Does this data suggest that hexatriene exhibits resonance structures?arrow_forward
- Consider the molecules of furan and benzene. The dominant Lewis structure of furan and the two resonance structures of benzene are shown below: Furan H X Benzene Compare the C-C bonds in benzene to the C-C bonds in furan. Based on the given structures, which one of the following dual statements is correct? In furan, the C-C bonds have different lengths: one is longer than the other two. In benzene, all six C-C bonds have equal lengths. In furan, the C-C bonds have different lengths: one is shorter than the other two. In benzene, all six C-C bonds have equal lengths. In furan, all three C-C bonds have equal lengths. In benzene, all six C-C bonds also have equal lengths. In furan, all three C-C bonds have equal lengths. In benzene, the C-C bonds have different lengths: three are longer than the other three. In furan, the C-C bonds have different lengths: one is longer than the other two. In benzene, the C-C bonds have different lengths: three are longer than the other three.arrow_forwardBe sure to answer all parts.Using the periodic table only, arrange the members of each of the following sets in order of increasing bond strength:(a) Br―Br, Cl―Cl, I―I (b) S―H, S―Br, S―Clarrow_forwardSome chemists believe that satisfaction of the octet rule should be the top criterion for choosing the dominant Lewis structure of a molecule or ion. Other chemists believe that achieving the best formal charges should be the top criterion. Consider the dihydrogen phosphate ion, HaPO, , in which the H atoms are bonded to O atoms. (a) What is the predicted dominant Lewis structure if satisfying the octet rule is the top eriterion? (b) What is the predicted dominant Lewis structure if achieving the best formal charges is the top criterion?arrow_forward
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